全球猫肠道微生物群的功能分析。

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Ostaizka Aizpurua, Amanda Bolt Botnen, Raphael Eisenhofer, Iñaki Odriozola, Luisa Santos-Bay, Mads Bjørn Bjørnsen, M. Thomas P. Gilbert, Antton Alberdi
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引用次数: 0

摘要

要想成功适应野生生活方式,获得不同的食物、住所和其他资源,需要快速的生理和行为改变,而肠道微生物群的可塑性可能会促进这种改变。为了研究肠道微生物群的改变是否支持这种向野生生活方式的转变,我们使用基因组解析宏基因组学分析了来自六个不同地理位置的家猫和野猫的肠道微生物组。通过重建来自92只猫的229个非冗余元基因组组装基因组,我们确定了一个典型的食肉动物微生物组结构,具有显著的多样性和不同地区的分类差异。虽然家猫和野猫的总体多样性指标没有显著差异,但考虑到地理和性别协变量的物种群落分层模型显示,野猫的微生物功能能力明显更大。氨基酸和脂肪降解能力的增加与野猫对粗蛋白质和粗脂肪的依赖相对应。第二项建模分析使用行为表型作为主要预测因子,揭示了短链脂肪酸、神经递质和维生素的微生物生产与猫的攻击性之间的正相关关系,这表明肠道微生物可能有助于提高野猫的攻击性和难以捉摸性。因此,功能性微生物组的变化可能在有利于野生生活方式的生理和行为特征的发展中发挥重要作用,这一假设值得通过微生物群操纵实验来验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Functional Insights Into the Effect of Feralisation on the Gut Microbiota of Cats Worldwide

Functional Insights Into the Effect of Feralisation on the Gut Microbiota of Cats Worldwide

Successfully adapting to a feral lifestyle with different access to food, shelter and other resources requires rapid physiological and behavioural changes, which could potentially be facilitated by gut microbiota plasticity. To investigate whether alterations in gut microbiota support this transition to a feral lifestyle, we analysed the gut microbiomes of domestic and feral cats from six geographically diverse locations using genome-resolved metagenomics. By reconstructing 229 non-redundant metagenome-assembled genomes from 92 cats, we identified a typical carnivore microbiome structure, with notable diversity and taxonomic differences across regions. While overall diversity metrics did not differ significantly between domestic and feral cats, hierarchical modelling of species communities, accounting for geographic and sex covariates, revealed significantly larger microbial functional capacities among feral cats. The increased capacity for amino acid and lipid degradation corresponds to feral cats' dietary reliance on crude protein and fat. A second modelling analysis, using behavioural phenotype as the main predictor, unveiled a positive association between microbial production of short-chain fatty acids, neurotransmitters and vitamins and cat aggressiveness, suggesting that gut microbes might contribute to heightened aggression and elusiveness observed in feral cats. Functional microbiome shifts may therefore play a significant role in the development of physiological and behavioural traits advantageous for a feral lifestyle, a hypothesis that warrants validation through microbiota manipulation experiments.

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来源期刊
Molecular Ecology
Molecular Ecology 生物-进化生物学
CiteScore
8.40
自引率
10.20%
发文量
472
审稿时长
1 months
期刊介绍: Molecular Ecology publishes papers that utilize molecular genetic techniques to address consequential questions in ecology, evolution, behaviour and conservation. Studies may employ neutral markers for inference about ecological and evolutionary processes or examine ecologically important genes and their products directly. We discourage papers that are primarily descriptive and are relevant only to the taxon being studied. Papers reporting on molecular marker development, molecular diagnostics, barcoding, or DNA taxonomy, or technical methods should be re-directed to our sister journal, Molecular Ecology Resources. Likewise, papers with a strongly applied focus should be submitted to Evolutionary Applications. Research areas of interest to Molecular Ecology include: * population structure and phylogeography * reproductive strategies * relatedness and kin selection * sex allocation * population genetic theory * analytical methods development * conservation genetics * speciation genetics * microbial biodiversity * evolutionary dynamics of QTLs * ecological interactions * molecular adaptation and environmental genomics * impact of genetically modified organisms
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